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早发性路易体痴呆与晚发性路易体痴呆和早发性阿尔茨海默病的临床表现比较。

Clinical Manifestations of Early-Onset Dementia With Lewy Bodies Compared With Late-Onset Dementia With Lewy Bodies and Early-Onset Alzheimer Disease.

机构信息

Department of Neurology, National Neuroscience Institute, Singapore General Hospital, Singapore.

Health Services Research and Biostatistics Unit, Singapore General Hospital, Singapore.

出版信息

JAMA Neurol. 2022 Jul 1;79(7):702-709. doi: 10.1001/jamaneurol.2022.1133.

Abstract

IMPORTANCE

Early-onset dementia, presenting in individuals younger than 65 years, is a diagnosis with significant social and financial implications. The early-onset form of dementia with Lewy bodies (DLB) is poorly understood.

OBJECTIVE

To investigate clinical features that distinguish early-onset DLB (onset and diagnosis at age <65 years) from late-onset DLB (onset at age ≥65 years) and from early-onset Alzheimer disease (AD) dementia.

DESIGN, SETTING, AND PARTICIPANTS: This is a retrospective case-control study on patients with pathologically confirmed DLB or AD enrolled in the National Alzheimer's Coordinating Center database from January 2005 to July 2017. The National Alzheimer's Coordinating Center Uniform Data Set comprised deidentified data collected by Alzheimer disease centers in the United States. Of patients fulfilling criteria for all-cause dementia at enrollment (n = 1152), those who at post mortem received a pathological diagnosis of either AD (n = 848) or Lewy body disease (n = 218) were selected. Excluding 52 patients owing to missing data and 12 diagnosed with Parkinson disease dementia, remaining patients were classified by age of symptom onset into early-onset AD, early-onset DLB, and late-onset DLB subgroups. Data were analyzed from June to December 2018 and from November to December 2021.

EXPOSURES

Demographics, cognitive, behavioral, and motor features recorded at first clinic visit and neuropathological characteristics at autopsy were analyzed by disease subgroup.

MAIN OUTCOMES AND MEASURES

Concordance between initial etiologic diagnosis of dementia and final pathological diagnosis was assessed, as was time to death.

RESULTS

A total of 542 individuals were categorized as having early-onset AD (n = 363; mean [SD] age, 53.0 [5.8] years; 208 [57.3%] male), early-onset DLB (n = 32; mean [SD] age, 57.9 [3.2] years; 23 [71.9%] male), and late-onset DLB (n = 147; mean [SD] age, 73.5 [5.5] years; 103 [70.1%] male). Early-onset DLB was clinically misdiagnosed in 16 individuals (50%). Features that predicted a diagnosis of early-onset DLB over early-onset AD included visual hallucinations (15 [46.9%] vs 42 [11.6%]), slowness (23 [71.9%] vs 95 [26.2%]), apathy (23 [71.9%] vs 189 [52.1%]), and motor deterioration that preceded cognitive and behavioral symptoms (7 [21.9%] vs 6 [1.7%]). Late-onset DLB had more amnestic features, but this was accounted for by a higher proportion of neocortical neuritic plaques and diffuse plaques (frequent in 79 [53.7%] vs 8 [25%]) than seen in early-onset DLB.

CONCLUSIONS AND RELEVANCE

This study found that early-onset DLB has clinical features that distinguish it from early-onset AD, whereas features of late-onset DLB are associated with a higher burden of AD copathology.

摘要

重要性

早发性痴呆,即在 65 岁以下人群中出现的诊断,具有重大的社会和经济影响。路易体痴呆(DLB)的早发型形式尚未被充分了解。

目的

研究区分早发性 DLB(发病和诊断年龄<65 岁)与晚发性 DLB(发病年龄≥65 岁)以及早发性阿尔茨海默病(AD)痴呆的临床特征。

设计、地点和参与者:这是一项回顾性病例对照研究,研究对象为 2005 年 1 月至 2017 年 7 月期间在国家阿尔茨海默病协调中心数据库中登记的经病理证实的 DLB 或 AD 患者。国家阿尔茨海默病协调中心统一数据集包括美国阿尔茨海默病中心收集的匿名数据。在所有病因性痴呆登记时(n=1152),符合标准的患者中,死后病理诊断为 AD(n=848)或路易体病(n=218)的患者被选择。排除因缺失数据(n=52)和诊断为帕金森病痴呆(n=12)的 52 例患者,剩余患者根据症状发病年龄分为早发性 AD、早发性 DLB 和晚发性 DLB 亚组。数据分析于 2018 年 6 月至 12 月和 2021 年 11 月至 12 月进行。

暴露

首次就诊时记录的人口统计学、认知、行为和运动特征以及尸检时的神经病理学特征按疾病亚组进行分析。

主要结果和测量

评估初始病因性痴呆诊断与最终病理诊断的一致性,以及死亡时间。

结果

共有 542 人被归类为早发性 AD(n=363;平均[标准差]年龄 53.0[5.8]岁;208[57.3%]为男性)、早发性 DLB(n=32;平均[标准差]年龄 57.9[3.2]岁;23[71.9%]为男性)和晚发性 DLB(n=147;平均[标准差]年龄 73.5[5.5]岁;103[70.1%]为男性)。早发性 DLB 在临床上被误诊了 16 例(50%)。预测早发性 DLB 诊断而非早发性 AD 的特征包括视觉幻觉(15[46.9%] vs 42[11.6%])、动作缓慢(23[71.9%] vs 95[26.2%])、冷漠(23[71.9%] vs 189[52.1%])以及认知和行为症状之前的运动恶化(7[21.9%] vs 6[1.7%])。晚发性 DLB 有更多的遗忘症状,但这归因于更多的皮质神经元纤维缠结和弥散斑块(79[53.7%] vs 8[25%]常见)比早发性 DLB 更常见。

结论和相关性

本研究发现,早发性 DLB 具有区别于早发性 AD 的临床特征,而晚发性 DLB 的特征与 AD 共病负担增加有关。

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